- Develop and optimize oral solid dosage (OSD) formulations including tablets, capsules, and modified-release products.
- Conduct pre-formulation studies, excipient compatibility, and stability assessments.
- Scale-up and technology transfer of formulations from lab to pilot and commercial scale.
- Prepare and review technical documents including batch records, development reports, and regulatory submissions.
- Collaborate with cross-functional teams (QA, QC, Production, Regulatory) for smooth project execution.
- Ensure compliance with cGMP, ICH, and regulatory guidelines.
📌 Research Associate (Una)
🏢 Stanford Laboratories
📍 Una
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